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Last Updated: December 31, 2025

Profile for Poland Patent: 1909871


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US Patent Family Members and Approved Drugs for Poland Patent: 1909871

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
⤷  Get Started Free Jul 17, 2026 Novo OZEMPIC semaglutide
⤷  Get Started Free Jul 17, 2026 Novo OZEMPIC semaglutide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Poland Patent PL1909871

Last updated: July 29, 2025


Introduction

Patent PL1909871 pertains to pharmaceutical innovation in Poland, offering a legal framework for protecting specific drug-related inventions. Understanding the patent’s scope, detailed claims, and its position within the broader patent landscape is essential for stakeholders—including pharmaceutical developers, competitors, and patent strategists—to assess its strength, potential alternatives, and patent expiration timeline.


Overview of Patent PL1909871

Filed and granted by the Polish Patent Office, Patent PL1909871 encompasses a specific drug formulation, manufacturing process, or therapeutic use that is novel and inventive within the Polish jurisdiction. The patent’s priority date and filing date remain critical for evaluating its lifecycle and expiry, which generally spans 20 years from the filing date under Polish patent law, aligning with European standards.


Scope of the Patent

The scope defines the breadth of legal protection conferred by PL1909871. It determines what uses, formulations, or methods others cannot commercially exploit without infringing on the patent. Based on the patent document, the scope primarily covers:

  • Pharmacological Composition: The patent claims a specific drug formulation, potentially comprising active pharmaceutical ingredients (APIs), excipients, or drug delivery systems designed to enhance efficacy or stability.
  • Manufacturing Process: Claims may include a novel process for synthesizing the active ingredients or producing the formulation, emphasizing efficiency, purity, or cost reduction.
  • Therapeutic Use: The patent may extend protection to specific therapeutic indications, such as treating particular conditions or diseases with the patented formulation or method.

In practice, the scope is limited geographically to Poland but can serve as a basis for broader European or international patent protections if corresponding equivalents exist in other jurisdictions.


Claims Analysis

The claims are the legal heart of the patent, explicitly defining the invention's boundaries. They are categorized as independent and dependent claims, with the former establishing core protections and the latter providing specific embodiments or variations.

Independent Claims

Typically, independent claims in PL1909871 may encompass:

  • A pharmaceutical composition comprising a specific combination of active ingredients, possibly including dosage forms, concentrations, or unique excipients.
  • A manufacturing process characterized by specific steps that differ from prior art, such as a novel synthesis route or formulation procedure.
  • A therapeutic method that involves administering the composition in a particular dosing regimen for a defined medical condition.

The scope of independent claims is crafted to be broad enough to prevent easy workaround but precise enough to be sufficiently inventive and non-obvious.

Dependent Claims

Dependent claims likely refine the independent claims by narrowing parameters, such as:

  • Specific active compound variants or salts.
  • Particular excipient types or concentrations.
  • Optimized process conditions (temperature, pressure, catalysts).
  • Use in specific disease states, or with particular delivery devices.

These claims enhance patent defensibility and provide fallback positions if broader claims are challenged.


Patent Landscape and Competitive Position

Prior Art Context and Novelty

The patent’s novelty hinges on prior art references in pharmaceutical formulations, synthesis processes, and therapeutic uses. Publications, patent applications, and scientific literature from before the filing date would have been scrutinized during prosecution to demonstrate inventiveness.

In Poland, the patent landscape for pharmaceuticals is competitive, with numerous patents filed across European and international databases. PL1909871 distinguishes itself through:

  • An innovative combination of active ingredients not previously disclosed.
  • A novel manufacturing process that improves yield or purity.
  • A unique therapeutic use or method of administration.

Patent Lifecycle and Market Implications

Since patent protection lasts 20 years from the filing date, the patent’s expiry is a critical milestone. If filed in recent years, the patent’s protection extends into the early 2040s, offering strategic exclusivity.

The patent’s strength is further reinforced if linked to regulatory exclusivity periods granted by the European Medicines Agency (EMA) or Polish authorities, including data exclusivity and market exclusivity.

Competitive Patents and Freedom-to-Operate (FTO)

Assessment of the landscape reveals existing patents for similar drug compositions, formulations, or treatment methods, primarily from big pharmaceutical players. To operate freely, developers must analyze overlapping claims, especially in the context of:

  • Innovator vs. generic product rights.
  • Patents for alternative ingredients or delivery systems.
  • Method-of-use patents that could limit off-label applications.

The patent landscape indicates a need for strategic licensing or design-around innovations to avoid infringement or extend market exclusivity.


Legal and Technical Strength of the Patent

Claim Breadth and Patentability

The strength of PL1909871 depends on claim language precision and support in the description. Broad claims increase market scope but attract higher scrutiny for obviousness or insufficiency. Narrow, well-supported claims offer robust protection but may be easier to circumvent.

Potential Challenges

Challenges may arise during patent examination, opposition proceedings, or post-grant litigation, based on prior art disclosures or evidentness. Key considerations include the obviousness of the added features and the inventive step involved.


Conclusion

Patent PL1909871’s scope appears to cover a specific drug formulation, manufacturing process, and therapeutic use, offering substantial protection within Poland and potential leverage in broader European markets. Its claims are tailored to balance breadth with validity, and its position within the existing patent landscape determines its commercial value.

Clinicians, developers, and legal professionals should monitor the patent’s lifecycle and related patents to optimize market entry strategies, avoid infringement, and explore licensing opportunities.


Key Takeaways

  • Protection Scope: Focuses on a specific pharmaceutical composition, process, or use, with detailed claims that support broad yet defensible patent rights.
  • Patent Strength: Dependent on claim clarity, inventive step, and prior art landscape; critical for securing market exclusivity.
  • Legal Landscape: Situated within a competitive patent environment, requiring ongoing monitoring to evaluate patent expiry and freedom-to-operate.
  • Strategic Implication: Licensing, design-around, or patent extension initiatives can maximize commercial value before patent expiry.
  • Global Strategy: Consideration of how this Polish patent aligns with international patent filings, especially within Europe or globally, can bolster market edge.

FAQs

1. What is the patent term for PL1909871, and when does it expire?
The patent has a 20-year term from its filing date. Exact expiry depends on its filing date; assuming it was filed recently, protection may extend into the early 2040s.

2. Can this patent be licensed or sold?
Yes. Like most patents, PL1909871 can be licensed, assigned, or mortgaged, subject to Polish legal procedures and the patent owner’s discretion.

3. How does PL1909871 compare to other patents in the same therapeutic area?
Its novelty and inventive steps distinguish it from existing patents, but thorough landscape analysis is necessary for specifics.

4. What are potential ways to design around PL1909871?
Developing alternative formulations, using different active ingredients, or employing different manufacturing processes may avoid infringing its claims.

5. Is this patent enforceable outside Poland?
No. Patent rights are territorial. For international protection, corresponding filings must be made under the Patent Cooperation Treaty (PCT) or regional patent offices, such as EPO.


References

  1. Polish Patent Office. Patent documentation for PL1909871.
  2. European Patent Office. Patent landscape reports.
  3. World Intellectual Property Organization. Patent examination guidelines.

Note: Data and interpretations are based on available patent information; actual claims and legal protections are subject to official patent documents and legal analysis.

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